Gerstmann-Sträussler-Scheinker disease revisited: accumulation of covalently-linked multimers of internal prion protein fragments

Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-related proteinase K-resistant prion protein (resPrP(D)) assoc...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Acta Neuropathol Commun
Prif Awduron: Cracco, Laura, Xiao, Xiangzhu, Nemani, Satish K., Lavrich, Jody, Cali, Ignazio, Ghetti, Bernardino, Notari, Silvio, Surewicz, Witold K., Gambetti, Pierluigi
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2019
Pynciau:
Research
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6540574/
https://ncbi.nlm.nih.gov/pubmed/31142381
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-019-0734-2
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